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Study identifier: NCT05838599 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Combining Topical Imiquimod With Local Radiotherapy for Treatment of Mycosis Fungoides

Condition: Mycosis Fungoides  ·  Sponsor: Northwestern University

PhaseEARLY_Phase 1
Planned participants25
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

Mycosis fungoides (MF) is the most common subtype of cutaneous T cell lymphoma (MF) and presents as cutaneous patches, plaques, and tumors. Radiation therapy (RT) is a frequently pursued management option for CTCL, especially in patients with more advanced skin disease. Imiquimod stimulates a Th1 lymphocyte response with increased IL-2 and IFN-α, but also induces IFN-α, TNF-α, IL-1α, IL-6, and IL-8, thereby bridging both innate and adaptive immunity. Dosing of both radiotherapy (RT) and imiquimod are based on standard-of-care doses/frequencies for CTCL. The reason imiquimod topical is given for a week before giving RT is to prime innate immune activity for when RT is delivered. It is believed that this serves as an adjuvant for the CD8+ antitumor response generated by RT. The primary aim of this study is to assess the safety and efficacy of a combination local radiotherapy and topical imiquimod approach for the treatment of conventional (CD4+) MF.

This description comes directly from the study's public registry record.

Talk to the study team

Dermatology Clinical Trials Unit  ·  312-503-5944  ·  NUderm-research@northwestern.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Northwestern University Department of DermatologyChicago, Illinois, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05838599